Boehringer Ingelheim

Title: Study Physician, Oncology (Remote) Location: United States Requisition ID 33320 Experienced professionals - Full-Time - Remote Job Description: The Study Physician (SP) is a critical role within Clinical Development Oncology (CD Onc) to establish readily available medical support and consultancy for clinical trials within CD Onc by a qualified and clinically experienced physician. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. Duties & Responsibilities - Responsible for medical content of Clinical Trial Protocols (CTPs), in line with TDO, in collaboration with CTL, CPL, Patient Safety Physician, Medical Writer and other trial and evidence team members to ensure high medical quality CTP. - Responsible for medical input into CTP updates. - Strong contribution to trial risk-based quality management from medical perspective, by defining medically relevant critical data/processes, related risks, and its mitigation/monitoring strategies in the Integrated Quality and Risk Management Plan (IQRMP) as well as in risk discussions during trial conduct. - Medical responsibility as co-author for development of a robust Clinical Quality Monitoring Plan (CQMP) in line with the critical data, medical quality risks and related monitoring/ mitigations identified in IQRMP. - Responsible for providing medical input into definition of important protocol deviations (iPD), providing input for compilation and review of trial iPD list from medical perspective, and support trial team in deciding on iPDs from identified potential iPDs. - Responsible for execution of relevant clinical quality monitoring for Study Physician using aggregated data outputs as per trial CQMP, timely mitigation & escalation of identified risks & quality issues. - Takes medical responsibility for agile & adaptive risk based Clinical Quality Monitoring of critical data. - Supports close to real time clinical data medical oversight by using advanced technologies and systems. - Proactively addresses/communicates clinical quality issues in a collaborative environment. - Contributes to the timely preparation of medically relevant core trial documents and timely milestones. - Responsible for medical input into Data Management documentation for the trial, such as eCRF design by efficient translation of medical questions into electronic data capturing. - Responsible for “Information for CRF completion” (ICC), Data Review Plan (e.g., propose items such as data screening rules for automated data queries, automated or manual data checks for clinical data consistency), laboratory parameters specifications for the project, Data Transfer Agreement, central laboratory alerts etc. - Responsible for the medical content of Patient Information and Informed Consent, Trial Level Monitoring Manual, Trial Communication Plan, Trial Training Plan, Trial Statistical Analysis Plan (TSAP) etc. - Responsible for medical contribution to Patient Narrative preparation, Clinical Trial Report planning and review of medical sections of Clinical Trial Report. - Contributes to the medical content of responses to questions from regulators and Ethic Committees/IRBs. - Responsible for medical input to study and site feasibility in planning and execution, patient recruitment, and retention plans. - Responds to medical queries from Investigators, CROs and/or Sponsor team representatives and contributes to maintenance of trial FAQ log/list. - Builds network with experts and active contribution to site engagement. - Supports Endpoint Adjudication (EA), Data Monitoring Committee (DMC), Data Safety Monitoring Boards (DSMB) and Steering Committees (SC) (as applicable), by presenting medical content of study to the respective committees, responding to medical questions and by ensuring good quality of data from CQM perspective. - Provision of medical training at Country feasibility training, Trial Investigators Meetings or to Sponsor staff. - Responsible for medical review of and contribution to the content of Trial Newsletters. - Contributes to the scientific publication of trial data (If applicable). - Requirements - Physician (MD) (ideally with medical thesis), trained in a clinical setting, and minimum of four (4) years of active clinical practice experience; specialization in internal medicine or general practice is desirable. MD in Oncology is preferred. - Experience specifically in Oncology Clinical Development is preferred. - Experience in pharma industry or CRO in medical or project management functions (ideally in Clinical Development) is desirable - Ability to communicate directly and concisely while collaborating with key stakeholders. - Pronounced analytical skills and systematic and well-structured working style. - Pronounced presentation and training skills. - Capability to work proactively and with team spirit in an international environment and team. - Displays the ability to use digital technologies to access information, be creative, innovative, solve problems, communicate, navigate, learn & apply in a digital environment. - Excellent interpersonal, active listening, influencing skills and fluency in English, both written and spoken. Eligibility Requirements: - Must be legally authorized to work in the United States without restriction. - Must be willing to take a drug test and post-offer physical (if required). - Must be 18 years of age or older. - Compensation This position offers a base salary typically between $250,000 and $394,000.  The position may be eligible for a role specific discretionary bonus, relocation, and/or other compensation elements. We continuously review market data and may adjust salary ranges as needed in the future. Actual compensation will be based on job-related factors such as skills, experience, and qualifications, and other factors permitted by law. For an overview of our benefits please click here.

Title: SR AD, National Acct and Sales Retail - Remote in U.S. Location: Atlanta, Georgia, United States Full-Time Job Description: As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Senior Associate Director, National Acct and Sales Retail is responsible for the management of the assigned Customers and account managers. The incumbent will develop the retail strategy for their relevant channel of assigned customers, and the implementation of the Boehringer sales/marketing plan to assure maximum distribution and market penetration of Boehringer products. Responsibilities for this role include achieving net sales, profit, and market share goals, and delivering against customer KPIs. The incumbent will manage a team of account managers, across relevant portfolio of customers. This role will support the leadership of the sales functional by developing key internal relationships, as well as external. This position has responsibility for key additional projects which support the continued development and future strategy of the sales organization. Duties & Responsibilities - Works with and through assigned customers and Key Account Managers to ensure sales performance meets or exceeds annual Company sales and market share objectives. - Implements a sales strategy to be executed through their relevant channel and Key Account Managers. - Exercises fiscal control on allocated operating budgets across multiple customers. - Manages across multiple customers. - Responsible for setting of annual KPIS. - Works to improve to sales bench of the organization, with the Head of Sales. - Utilizes appropriate data sources to develop tactical plans and to develop future customer / channel strategy. - Actively monitors progress of work, cross-functional activities, and accountability. - Plans and executes meetings that effectively implement objectives and strategies as determined by the Company. - Spends appropriate amount of time developing customers, networks, and their relationships to foster Company business. - Leads the senior customer engagement strategy across the channel, ensuring relevant T2T, strategic customer meetings and line reviews are delivered. - Develops positive relationships with Company internal customers, such as supply, marketing, Segment Leads. - Performs all Company business in accordance with all regulations (e.g., EEO, FDA, OSHA, etc.) and Company policies and procedures. - Demonstrates high ethical and professional standards with all business contacts to maintain BIAH's excellent reputation within the community. - Leads special strategic projects as relevant, which will ensure future success of the retail sales team. Requirements - BS/BA. - Minimum of eight to ten (8-10) years successful commercial industry experience. - Minimum of five to seven (5-7) years retail experience, across Omni channel, ideally in US Mass market, E-commerce, or Retail Pharmacy. - Understanding of retail analytics, economics, supply chain, and consumer insights. - Understanding of the digital environment, e.g., E-Commerce and digital marketing. - Understanding of the US retail environment. - Experience in working cross-functionally. - Project Management Skills. - Proficiency in Excel, Word, Outlook, PowerPoint, and database applications. - Ability to travel. Eligibility Requirements: - Must be legally authorized to work in the United States without restriction. - Must be willing to take a drug test and post-offer physical (if required). - Must be 18 years of age or older.

Lead the planning and execution of meetings and events, establish policies and procedures for effective governance, and manage relationships with vendors while ensuring alignment with organizational goals and success metrics.

Title: Study Physician, Oncology Location:Ridgefield, CT , United States (Remote) Requisition ID 33320 Job Description: The Study Physician (SP) is a critical role within Clinical Development Oncology (CD Onc) to establish readily available medical support and consultancy for clinical trials within CD Onc by a qualified and clinically experienced physician. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development, and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in several ways to foster a healthy working environment, meaningful work, mobility, networking, and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. Duties & Responsibilities - Responsible for medical content of Clinical Trial Protocols (CTPs), in line with TDO, in collaboration with CTL, CPL, Patient Safety Physician, Medical Writer and other trial and evidence team members to ensure high medical quality CTP. - Responsible for medical input into CTP updates. - Strong contribution to trial risk-based quality management from medical perspective, by defining medically relevant critical data/processes, related risks, and its mitigation/monitoring strategies in the Integrated Quality and Risk Management Plan (IQRMP) as well as in risk discussions during trial conduct. - Medical responsibility as co-author for development of a robust Clinical Quality Monitoring Plan (CQMP) in line with the critical data, medical quality risks and related monitoring/ mitigations identified in IQRMP. - Responsible for providing medical input into definition of important protocol deviations (iPD), providing input for compilation and review of trial iPD list from medical perspective, and support trial team in deciding on iPDs from identified potential iPDs. - Responsible for execution of relevant clinical quality monitoring for Study Physician using aggregated data outputs as per trial CQMP, timely mitigation & escalation of identified risks & quality issues. - Takes medical responsibility for agile & adaptive risk based Clinical Quality Monitoring of critical data. - Supports close to real time clinical data medical oversight by using advanced technologies and systems. - Proactively addresses/communicates clinical quality issues in a collaborative environment. - Contributes to the timely preparation of medically relevant core trial documents and timely milestones. - Responsible for medical input into Data Management documentation for the trial, such as eCRF design by efficient translation of medical questions into electronic data capturing. - Responsible for “Information for CRF completion” (ICC), Data Review Plan (e.g., propose items such as data screening rules for automated data queries, automated or manual data checks for clinical data consistency), laboratory parameters specifications for the project, Data Transfer Agreement, central laboratory alerts etc. - Responsible for the medical content of Patient Information and Informed Consent, Trial Level Monitoring Manual, Trial Communication Plan, Trial Training Plan, Trial Statistical Analysis Plan (TSAP) etc. - Responsible for medical contribution to Patient Narrative preparation, Clinical Trial Report planning and review of medical sections of Clinical Trial Report. - Contributes to the medical content of responses to questions from regulators and Ethic Committees/IRBs. - Responsible for medical input to study and site feasibility in planning and execution, patient recruitment, and retention plans. - Responds to medical queries from Investigators, CROs and/or Sponsor team representatives and contributes to maintenance of trial FAQ log/list. - Builds network with experts and active contribution to site engagement. - Supports Endpoint Adjudication (EA), Data Monitoring Committee (DMC), Data Safety Monitoring Boards (DSMB) and Steering Committees (SC) (as applicable), by presenting medical content of study to the respective committees, responding to medical questions and by ensuring good quality of data from CQM perspective. - Provision of medical training at Country feasibility training, Trial Investigators Meetings or to Sponsor staff. - Responsible for medical review of and contribution to the content of Trial Newsletters. - Contributes to the scientific publication of trial data (If applicable). Requirements - Physician (MD) (ideally with medical thesis), trained in a clinical setting, and minimum of four (4) years of active clinical practice experience; specialization in internal medicine or general practice is desirable. MD in Oncology is preferred. - Experience specifically in Oncology Clinical Development is preferred. - Experience in pharma industry or CRO in medical or project management functions (ideally in Clinical Development) is desirable - Ability to communicate directly and concisely while collaborating with key stakeholders. - Pronounced analytical skills and systematic and well-structured working style. - Pronounced presentation and training skills. - Capability to work proactively and with team spirit in an international environment and team. - Displays the ability to use digital technologies to access information, be creative, innovative, solve problems, communicate, navigate, learn & apply in a digital environment. - Excellent interpersonal, active listening, influencing skills and fluency in English, both written and spoken Eligibility Requirements: - Must be legally authorized to work in the United States without restriction. - Must be willing to take a drug test and post-offer physical (if required). - Must be 18 years of age or older. Compensation This position offers a base salary typically between $250,000 and $394,000.  The position may be eligible for a role specific discretionary bonus, relocation, and/or other compensation elements. We continuously review market data and may adjust salary ranges as needed in the future. Actual compensation will be based on job-related factors such as skills, experience, and qualifications, and other factors permitted by law.

Title: Director, Experimental Medicine - Medical Writing - Remote Primary location: Ridgefield, CT, Connecticut, United States Remote: this position is considered remote based. As an employee of Boehringer Ingelheim, you will actively contribute to the discovery, development and delivery of our products to our patients and customers. Our global presence provides opportunity for all employees to collaborate internationally, offering visibility and opportunity to directly contribute to the companies' success. We realize that our strength and competitive advantage lie with our people. We support our employees in a number of ways to foster a healthy working environment, meaningful work, mobility, networking and work-life balance. Our competitive compensation and benefit programs reflect Boehringer Ingelheim's high regard for our employees. The Director of ExpMED Global Medical Writing is part of the ExpMED Global Medical Writing Leadership team and contributes to overall ExpMED global medical writing strategy including the organizational set up, development, implementation, and oversight of a high-performing, innovative medical writing group for the early phase, and the development and oversight of an ExpMED global medical writing excellence strategy (i.e., acceleration of clinical development timelines, use of AI, and creation of patient value while maintaining high quality) via strategic planning and execution of early clinical documents across all Therapeutic Areas. The Director of ExpMED Global Medical Writing provides leadership and guidance to a diverse team, creates an environment that inspires, motivates, and empowers colleagues, fosters a culture of continuous learning, knowledge sharing, improvement, innovation, accountability, and collaboration to accelerate clinical trial delivery and maximize value for investigational sites, patients, and the organization. Duties & Responsibilities • As part of the ExpMED Global Medical Writing Leadership team, accountable for the creation and continuous refinement of a world-class ExpMED Global Medical Writing department to effectively deliver. • As part of the ExpMED Global Medical Writing Leadership team, develop and implement a global ExpMED medical writing excellence strategy that simplifies processes, sharpens focus, and accelerates clinical development across all therapeutic areas. • Build and continuously enhance a high-performing and innovative team. • Accountable for talent attraction, development retention, functional talent development, and succession planning within ExpMED Global Medical Writing, in close alignment with HR. • Accountable for the creation of an environment that inspires, motivates, and empowers colleagues to accelerate clinical development timelines and to create value for patients and the healthcare system. • Accountable that staff is well trained and qualified; supports staff in technical and personal skills development to support career progression. • Leads the communication of scientific programs and holistic evidence to key stakeholders, including investigators, regulators, payers, patients, and caregivers. • Oversees capacity planning, financial management, and the strategic deployment of internal and external (CRO) resources to support clinical program needs. • Provide oversight to constantly improve processes and standards to prevent and/or remedy quality and/or compliance findings (in-house and/or CRO setting) to ensure early clinical execution excellence, in alignment with other Corporate functions. • Representation of Boehringer Ingelheim at external meetings and conferences to create value for Boehringer Ingelheim and external stakeholders. Requirements - MS, PhD Degree in the Life Sciences with a minimum of 10 years of experience as a medical writer or a similar role preparing regulated documents in the pharmaceutical and/or biotech industry and/or CRO. - AAI leadership competencies with >5 years in (ideally different) leadership roles. - Strong leadership skills with the ability to inspire and motivate to build a high-performing, innovative team. - Comprehensive understanding of drug development and reporting process required for study reports, submission documents, and data transparency deliverables across multiple providers. - Experience in (at least passion for) storytelling. - Knowledge of vendor processes, contracting, and best practices in outsourcing; ability to influence vendor improvements. - Demonstrated experience presenting to scientific and non-scientific audiences. - Experience managing multiple, complex projects, and a strong record of developing successful partnerships and meeting customer expectations in global settings. - Strategic mindset with the ability to drive innovation, digital transformation, and process integration across complex, global environments. - Expertise in globalizing functions to operate in a standardized fashion. - Excellent interpersonal, active listening, and influencing skills; establishes and maintains professional and productive working relationships with colleagues and vendors. - Proactively identify gaps, emerging risks, and opportunities for improvement through ongoing analysis and benchmarking to maintain industry leading position - Encourages the adoption of new technologies, smart risk-taking, and a unified identity that empowers teams and accelerates clinical development. - Demonstrated ability to build, lead, develop and maintain a high-performance, medical writing team. - Onsite/Flex*: This position is site based with flexibility for remote working. Working onsite a minimum of 2-3 days per week is required. Remote working norms will be clarified during the interview process. Eligibility Requirements: - Must be legally authorized to work in the United States without restriction. - Must be willing to take a drug test and post-offer physical (if required). - Must be 18 years of age or older. Compensation Data The base salary range for this position is $200,000.00 to $316,000.00 USD. The position may be eligible for a role specific discretionary bonus, relocation, and/or other compensation elements. We continuously review market data and may adjust salary ranges as needed in the future. Actual compensation will be based on job-related factors such as skills, experience, and qualifications, and other factors permitted by law. Our Company Boehringer Ingelheim is a biopharmaceutical company active in both human and animal health. As one of the industry’s top investors in research and development, the company focuses on developing innovative therapies that can improve and extend lives in areas of high unmet medical need. Independent since its foundation in 1885, Boehringer takes a long-term perspective, embedding sustainability along the entire value chain. Our approximately 54,500 employees serve over 130 markets to build a healthier and more sustainable tomorrow. Learn more at www.boehringer-ingelheim.com Why Boehringer Ingelheim? With us, you can develop your own path in a company with a culture that knows our differences are our strengths – and break new ground in the drive to make millions of lives better. Here, your development is our priority. Supporting you to build a career as part of a workplace that is independent, authentic and bold, while tackling challenging work in a respectful and friendly environment where everyone is valued and welcomed. Alongside, you have access to programs and groups that ensure your health and wellbeing are looked after – as we make major investments to drive global accessibility to healthcare. By being part of a team that is constantly innovating, you’ll be helping to transform lives for generations. Want to learn more? Visit https://www.boehringer-ingelheim.com/us/careers Explore our total rewards here: Visit https://www.boehringer-ingelheim.com/us/careers/benefits-rewards All qualified applicants will receive consideration for employment without regard to a person’s actual or perceived race, including natural hairstyles, hair texture and protective hairstyles; color; creed; religion; national origin; age; ancestry; citizenship status; marital status; sex or gender (including pregnancy, childbirth or related medical condition); gender identity or gender expression (including transgender status); sexual orientation; disability; protected medical condition as defined by applicable state or local law; military service and veteran status; genetic information (including the refusal to submit to genetic testing); or any other class or characteristic protected by applicable federal, state or local laws and ordinances.

• Lead clinical delivery and provide operational input into late-phase Clinical Development Plans (CDPs) • Develop and oversee operational strategies, timelines, country and site selection, and sourcing models across assets • Partner with cross-functional stakeholders to ensure consistency, efficiency, and avoidance of redundancy across trials • Drive adoption of innovative trial designs, digital technologies, and data-driven decision-making • Ensure patient-centric approaches and sustained expert engagement throughout the development lifecycle • Share performance feedback with Study Operations Team for assigned trial team members